1. BLM helicase unwinds lagging strand substrates to assemble the ALT telomere damage response.
- Author
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Jiang H, Zhang T, Kaur H, Shi T, Krishnan A, Kwon Y, Sung P, and Greenberg RA
- Subjects
- Humans, DNA, Single-Stranded metabolism, DNA, Single-Stranded genetics, X-linked Nuclear Protein genetics, X-linked Nuclear Protein metabolism, DNA Helicases metabolism, DNA Helicases genetics, Bloom Syndrome genetics, Bloom Syndrome metabolism, Bloom Syndrome enzymology, Bloom Syndrome pathology, Cell Line, Tumor, RecQ Helicases metabolism, RecQ Helicases genetics, Telomere Homeostasis, Telomere metabolism, Telomere genetics, DNA Replication, DNA Damage
- Abstract
The Bloom syndrome (BLM) helicase is critical for alternative lengthening of telomeres (ALT), a homology-directed repair (HDR)-mediated telomere maintenance mechanism that is prevalent in cancers of mesenchymal origin. The DNA substrates that BLM engages to direct telomere recombination during ALT remain unknown. Here, we determine that BLM helicase acts on lagging strand telomere intermediates that occur specifically in ALT-positive cells to assemble a replication-associated DNA damage response. Loss of ATRX was permissive for BLM localization to ALT telomeres in S and G2, commensurate with the appearance of telomere C-strand-specific single-stranded DNA (ssDNA). DNA2 nuclease deficiency increased 5'-flap formation in a BLM-dependent manner, while telomere C-strand, but not G-strand, nicks promoted ALT. These findings define the seminal events in the ALT DNA damage response, linking aberrant telomeric lagging strand DNA replication with a BLM-directed HDR mechanism that sustains telomere length in a subset of human cancers., Competing Interests: Declaration of interests R.A.G. is a co-founder and scientific advisory board member of RADD Pharmaceuticals and a scientific advisory board member for Dong-A ST Co. Neither engagement directly relates to the substance of this study., (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Published
- 2024
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